Experience

Prime Matter Labs
• United States
• Manufacturing
• 1 - 100 Employee
• Process Scientist

  • Apr 2023 - Present


PakLab

• United States
• Personal Care Product Manufacturing
• 1 - 100 Employee

• Process Development Scientist

  • Jan 2015 - Apr 2023

• Process Development Scientist

  • Jan 2015 - Apr 2023

• Process Scientist

  • Jan 2015 - Apr 2023

  Develops manufacturing processes by studying product requirements; researching, designing, modifying, and testing manufacturing methods and equipment; conferring with equipment vendors. Improves manufacturing efficiency by analyzing and planning work flow, space requirements, and equipment layout. Preform Stability & Compatibility studies by evaluating lab formulated products under the influence of a variety of environmental factors such as temperature, humidity, light and final… Show more Develops manufacturing processes by studying product requirements; researching, designing, modifying, and testing manufacturing methods and equipment; conferring with equipment vendors. Improves manufacturing efficiency by analyzing and planning work flow, space requirements, and equipment layout. Preform Stability & Compatibility studies by evaluating lab formulated products under the influence of a variety of environmental factors such as temperature, humidity, light and final packaging component to ensure that the cosmetic product maintains its intended physical, chemical and microbiological quality, as well as functionality and aesthetics when stored under appropriate conditions.



Johnson & Johnson

• Law Practice
• 1 - 100 Employee

• Pilot Plant specialist

  • Sep 2012 - Jun 2014

  Performed preliminary study of cosmetic products conducted in small scale manufacturing kettles in order to evaluate feasibility, time, cost, adverse events, and improve the study design prior to performance of a full-scale manufacturing. Technical Transfer role to demonstrate specific procedures and points of concern for process to contribute to smooth transfers for full-scale manufacturing.

• GMP Laboratories Coordinater

  • Mar 2011 - Sep 2012


BioScreen Testing Services
• United States
• Biotechnology Research
• 1 - 100 Employee
• QA Specialist

  • 2010 - 2011


McGuff Company, Inc.

• United States
• Pharmaceutical Manufacturing
• 1 - 100 Employee

• Quality Assurance Specialist

  • Feb 2008 - 2010

  Reviewed and released finished product and raw materials according to specification. Conducted internal audits of finished cGMP paperwork and proper archiving of records. Submitted testing samples of raw materials and finished product to external testing laboratories. Reviewed and released samples that met specifications and archived the results according to cGMP procedures. Preformed investigations on any deviation from cGMP procedures which included Non-Conformance (NC)… Show more Reviewed and released finished product and raw materials according to specification. Conducted internal audits of finished cGMP paperwork and proper archiving of records. Submitted testing samples of raw materials and finished product to external testing laboratories. Reviewed and released samples that met specifications and archived the results according to cGMP procedures. Preformed investigations on any deviation from cGMP procedures which included Non-Conformance (NC), Out-of-Specification (OOS), or Out-of-Trend (OOT) that sometimes led to a Corrective and Preventative Action (CAPA) that was implemented. Show less Reviewed and released finished product and raw materials according to specification. Conducted internal audits of finished cGMP paperwork and proper archiving of records. Submitted testing samples of raw materials and finished product to external testing laboratories. Reviewed and released samples that met specifications and archived the results according to cGMP procedures. Preformed investigations on any deviation from cGMP procedures which included Non-Conformance (NC)… Show more Reviewed and released finished product and raw materials according to specification. Conducted internal audits of finished cGMP paperwork and proper archiving of records. Submitted testing samples of raw materials and finished product to external testing laboratories. Reviewed and released samples that met specifications and archived the results according to cGMP procedures. Preformed investigations on any deviation from cGMP procedures which included Non-Conformance (NC), Out-of-Specification (OOS), or Out-of-Trend (OOT) that sometimes led to a Corrective and Preventative Action (CAPA) that was implemented. Show less